Literature DB >> 25331681

Molecular signalings in keloid disease and current therapeutic approaches from natural based compounds.

Thitita Unahabhokha1, Apirada Sucontphunt, Ubonthip Nimmannit, Pithi Chanvorachote, Nuttida Yongsanguanchai, Varisa Pongrakhananon.   

Abstract

CONTEXT: Keloid is an excessive dermal scar occurring in response to skin injuries. Several therapeutic strategies have been proposed to ease the aggressiveness of keloid scarring. Even though the principle mechanism underlying the disease propagation still remains unidentified, several signaling pathways were highly focused as plausible pathways involving keloid formation, including transforming growth factor-beta 1 (TGF-β1), mitogen-activated protein kinase (MAPK), insulin-like growth factor-I (IGF-I), and integrin pathways. Natural compounds containing multiple bioeffective properties such as quercetin, asiaticoside, Astragalus membranaceus Bunge. (Leguminosae), and Salvia miltiorrhiza Bunge. (Lamiaceae) extracts, curcuminoids, oxymatrine, madecassoside, and Aneilema keisak Hassk. (Commelinaceae) are claimed as candidates for therapeutic treatment against keloid disorder.
OBJECTIVE: This review investigates current mechanisms regarding keloid formation and provides scientific evidence supporting the therapeutic potential of natural compounds.
METHODS: This review obtained and analyzed a number of literature data items from various databases including Pubmed, ScienceDirect, and Elton B. Stephens Company (EBSCO). RESULT: Several phytochemical compounds are able to suppress keloid scar development through manipulating various components in the complex signaling cascades.
CONCLUSION: The present review may be helpful to future studies that further examine the molecular mechanism of keloid etiology as well as investigate the anti-keloid property in natural compounds.

Entities:  

Keywords:  Anti-keloid; collagen production; fibroblast; insulin-like growth factor-I; integrin Smad; mitogen-activated protein kinase; transforming growth factor-β1

Mesh:

Substances:

Year:  2014        PMID: 25331681     DOI: 10.3109/13880209.2014.918157

Source DB:  PubMed          Journal:  Pharm Biol        ISSN: 1388-0209            Impact factor:   3.503


  17 in total

1.  Long non-coding RNA HOXA11-AS accelerates the progression of keloid formation via miR-124-3p/TGFβR1 axis.

Authors:  Jun Jin; Zhen-Hua Jia; Xiao-Hua Luo; Hong-Feng Zhai
Journal:  Cell Cycle       Date:  2019-12-27       Impact factor: 4.534

Review 2.  Promising Natural Products in New Drug Design, Development, and Therapy for Skin Disorders: An Overview of Scientific Evidence and Understanding Their Mechanism of Action.

Authors:  Nurul Amirah Mohd Zaid; Mahendran Sekar; Srinivasa Reddy Bonam; Siew Hua Gan; Pei Teng Lum; M Yasmin Begum; Nur Najihah Izzati Mat Rani; Jaishree Vaijanathappa; Yuan Seng Wu; Vetriselvan Subramaniyan; Neeraj Kumar Fuloria; Shivkanya Fuloria
Journal:  Drug Des Devel Ther       Date:  2022-01-06       Impact factor: 4.162

Review 3.  MicroRNA-21 in Skin Fibrosis: Potential for Diagnosis and Treatment.

Authors:  Yan Li; Juan Zhang; Yuying Lei; Lechun Lyu; Ruiling Zuo; Ting Chen
Journal:  Mol Diagn Ther       Date:  2017-12       Impact factor: 4.074

4.  Peroxisome proliferator-activated receptor-γ agonist inhibits collagen synthesis in human keloid fibroblasts by suppression of early growth response-1 expression through upregulation of miR-543 expression.

Authors:  Hua-Yu Zhu; Wen-Dong Bai; Hong-Tao Wang; Song-Tao Xie; Ke Tao; Lin-Lin Su; Jia-Qi Liu; Xue-Kang Yang; Jun Li; Yun-Chuan Wang; Ting He; Jun-Tao Han; Da-Hai Hu
Journal:  Am J Cancer Res       Date:  2016-06-01       Impact factor: 6.166

5.  Increased Cthrc1 Activates Normal Fibroblasts and Suppresses Keloid Fibroblasts by Inhibiting TGF-β/Smad Signal Pathway and Modulating YAP Subcellular Location.

Authors:  Meng-Jie Zhao; Si-Yuan Chen; Xiao-Ying Qu; Bilal Abdul-Fattah; Ting Lai; Meng Xie; Shi-di Wu; You-Wen Zhou; Chang-Zheng Huang
Journal:  Curr Med Sci       Date:  2018-10-20

Review 6.  Scientific landscape and trend analysis of keloid research: a 30-year bibliometric review.

Authors:  Yuming Chong; Xiao Long; Yuh-Shan Ho
Journal:  Ann Transl Med       Date:  2021-06

7.  Human adipose-derived stem cells inhibit bioactivity of keloid fibroblasts.

Authors:  Xiuxia Wang; Yan Ma; Zhen Gao; Jun Yang
Journal:  Stem Cell Res Ther       Date:  2018-02-21       Impact factor: 6.832

8.  Profibrogenic effect of high-mobility group box protein-1 in human dermal fibroblasts and its excess in keloid tissues.

Authors:  Won Jai Lee; Seung Yong Song; Hyun Roh; Hyo Min Ahn; Youjin Na; Jihee Kim; Ju Hee Lee; Chae Ok Yun
Journal:  Sci Rep       Date:  2018-05-30       Impact factor: 4.379

9.  LncRNA H19 promotes keloid formation through targeting the miR-769-5p/EIF3A pathway.

Authors:  Lingang Xu; Nan Sun; Guangshuai Li; Linbo Liu
Journal:  Mol Cell Biochem       Date:  2021-01-03       Impact factor: 3.396

10.  Reductive metabolism of oxymatrine is catalyzed by microsomal CYP3A4.

Authors:  Wenqin Liu; Jian Shi; Lijun Zhu; Lingna Dong; Feifei Luo; Min Zhao; Ying Wang; Ming Hu; Linlin Lu; Zhongqiu Liu
Journal:  Drug Des Devel Ther       Date:  2015-10-30       Impact factor: 4.162

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